Classifications

• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
  • C08F10/00—Homopolymers and copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
  • C08F110/00—Homopolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond
  • C08F110/04—Monomers containing three or four carbon atoms
  • C08F110/06—Propene

Definitions

• the present invention relates to a process for preparing an aqueous polymer dispersion by polymerization of at least one olefinically unsaturated compound (monomer) in an aqueous medium in the presence of at least one dispersant, wherein the polymerization is carried out in the presence of a solid polymerization catalyst.
• the invention further relates to the aqueous polymer dispersions obtainable by the process of the present invention and also to their use as binders in adhesives, sealants, polymer-based plasters and renders, paper coating compositions and paints.
• Aqueous polymer dispersions are generally known. These are fluid systems comprising polymer tangles (referred to as polymer particles) consisting of a plurality of intertwined polymer chains dispersed as disperse phase in an aqueous dispersion medium.
• the weight average diameter of the polymer particles is frequently in the range from 10 to 5000 nm.
• aqueous polymerization dispersions Like polymerization solutions when the solvent is evaporated, aqueous polymerization dispersions have the potential of forming polymer films on evaporation of the aqueous dispersion medium, which is why they are employed, in particular, as binders. Owing to their environmentally friendly properties, they are gaining increasing importance.
• aqueous polymer dispersions are frequently carried out by free-radical-initiated aqueous emulsion polymerization [cf. for example, Encyclopedia of Polymer Science and Engineering, Vol. 8, page 659 ff. (1987); D.C. Blackley, in High Polymer Latices, Vol. 1, page 35 ff. (1966); H. Warson, The Applications of Synthetic Resin Emulsions, page 246 ff., chapter 5 (1972); D. Diederich, Chemie in shu Zeit 24, pages 135 to 142 (1990); Emulsion Polymerisation, Interscience Publishers, New York (1965); DE-A 40 03 422 and Dispersionen synthetischer Hochpolymerer, F. Hölscher, Springer-Verlag, Berlin 1969].
• free-radical initiators are used as polymerization “catalysts” and polar monomers are generally used as main monomers.
• Nonpolar monomers are particularly suitable for these polymerization processes. If they are used at all, polar monomers are used to only a minor extent for modifying the polymer properties.
• the polymerization catalysts used for these polymerization processes are, in particular, catalytically active transition metal complexes or transition metal complexes in combination with compounds, known as activators, which activate the transition metal complexes.
• these polymerization reactions are usually carried out in the form of a bulk polymerization in which the monomer is simultaneously reactant and solvent or in the form of a solution polymerization in which the transition metal complex or the transition metal complex/activator combination, the monomer and the polymer formed are all present in solution in a nonaqueous frequently aprotic organic solvent.
• these transition metal complexes or transition metal complex/activator combinations homogeneously dissolved in the monomer, solvent or generally in the polymerization medium are referred to as “homogeneous polymerization catalysts”.
• conjugated dienes such as butadiene can also be polymerized by an insertion mechanism in an aqueous medium using hydrolysis-stable transition metal complexes or transition metal complex/activator combinations [cf., for example, Ono and Kato, J. Polym. Sci. A. 2000, 38, pages 1083 to 1089, Rinehart, J. Polym. Sci. C. 1969, 27, pages 7 to 25, and also DE-A 2332921].
• DE-A 19859191 discloses the ring-opening polymerization of cyclic olefins in an aqueous medium using hydrolysis-stable transition metal complexes or transition metal complex/activator combinations.
• a disadvantage of these “non-free-radical” polymerization processes is that the transition metal complexes used as polymerization catalysts, which are frequently expensive noble metal compounds, remain molecularly dissolved in the aqueous polymer dispersion and can thus only be used once.
• the transition metal complexes remaining in the aqueous polymer dispersions can interfere in later use, for example in polymer film formation, or contribute to discoloration of the polymer films formed.
• Suitable solid polymerization catalysts are in principle all solid polymerization catalysts which are able to trigger and maintain a polymerization reaction of olefinically unsaturated compounds in an aqueous medium.
• solid polymerization catalysts are polymerization catalysts which have a solubility of ⁇ 0.1% by weight, frequently ⁇ 0.05% by weight and often ⁇ 0.01% by weight, in deionized water at 20° C.
• the solid polymerization catalysts can in principle have any shape and size, for example they can be in the form of cylinders, rings, spheres, hollow bodies, gauzes, woven meshes or amorphous particles.
• the solid polymerization catalysts are frequently in the form of amorphous and/or porous particles having a mean particle diameter in the range from 1 ⁇ m to 10 cm, often in the range from 10 ⁇ m to 1 cm or in the range from 30 ⁇ m to 1000 ⁇ m.
• possible ethylenically unsaturated compounds include both pure ethylenically unsaturated hydrocarbon compounds and heteroatom-containing ⁇ -olefins, e.g. (meth)acrylic esters and homoallyl or allyl alcohols, ethers or halides.
• Pure ethylenically unsaturated hydrocarbons which are useful are C 2 -C 20 -1-alkenes.
• low molecular weight alkenes for example ethene, and ⁇ -alkenes having from 3 to 20 carbon atoms, e.g.
• cyclic olefins such as cyclopentene, cyclohexene or norbornene, conjugated dienes such as 1,3-butadiene (butadiene), 2-chlorobutadiene, 2-methylbutadiene or 2,3-dimethylbutadiene, aromatic olefin compounds such as styrene, ⁇ -methylstyrene or ortho-, meta- or para-vinyltoluene and vinyl esters such as vinyl acetate or vinyl propionate.
• cyclic olefins such as cyclopentene, cyclohexene or norbornene, conjugated dienes such as 1,3-butadiene (butadiene), 2-chlorobutadiene, 2-methylbutadiene or 2,3-dimethylbutadiene, aromatic olefin compounds such as styrene, ⁇ -methylstyrene or ortho-, meta- or para-vinyltoluene
• C 2 -C 20 -1-alkenes are particularly suitable.
• the monomers mentioned generally constitute the main monomers which make up a proportion of >50% by weight, in particular ⁇ 80% by weight or ⁇ 90% by weight, of the total amount of monomers.
• the monomer mixture to be polymerized frequently consists of 100% by weight of at least one of the abovementioned monomers.
• the monomers containing amide or acid groups are normally present only as modifying monomers in amounts of from ⁇ 50% by weight, ⁇ 10% by weight, preferably ⁇ 5% by weight, in each case based on the total amount of monomers.
• the process of the present invention is carried out using at least one dispersant which keeps the polymer particles formed during the polymerization dispersed in the aqueous phase and thus ensures the stability of the aqueous polymer dispersion produced.
• the respective solid polymerization catalyst is very finely divided, for example has a particle size of from 1 to 10 ⁇ m, the solid polymerization catalyst particles are also kept dispersed in the aqueous phase.
• dispersant it is possible to use both protective colloids and emulsifiers.
• Suitable protective colloids are, for example, polyvinyl alcohols, polyalkylene glycols, alkali metal salts of polyacrylic acids and polymethacrylic acids, cellulose, starch and gelatin derivatives or copolymers comprising acrylic acid, methacrylic acid, maleic anhydride, 2-acrylamido-2-methylpropanesulfonic acid and/or 4-styrenesulfonic acid and alkali metal salts thereof and also homopolymers and copolymers comprising N-vinylpyrrolidone, N-vinylcaprolactam, N-vinylcarbazole, 1-vinylimidazole, 2-vinylimidazole, 2-vinylpyridine, 4-vinylpyridine, acrylamide, methacrylamide, and acrylates, methacrylates, acrylamides and/or methacrylamides bearing amine groups.
• emulsifiers and/or protective colloids are frequently exclusively emulsifiers whose relative molecular weights are, unlike the protective colloids, usually below 1500. They can be either anionic, cationic or nonionic in nature. If mixtures of surface-active substances are used, it is self-evident that the individual components have to be compatible with one another, which in the case of doubt can be checked by means of a few preliminary tests. In general, anionic emulsifiers are compatible with one another and with nonionic emulsifiers. The same applies to cationic emulsifiers, while anionic and cationic emulsifiers are usually not compatible with one another.
• Nonionic emulsifiers which can be used are, for example, ethoxylated monoalkylphenols, dialkylphenols and trialkylphenols (EO units: 3 to 50, alkyl radical: C 4 to C 12 ) and ethoxylated fatty alcohols (EO units: 3 to 80; alkyl radical: C 8 to C 36 ).
• emulsifiers examples include the Lutensol® A grades (C 12 C 14 -fatty alcohol ethoxylates, EO units: 3 to 8), Lutensol® AO grades (C 13 C 15 oxo alcohol ethoxylates, EO units: 3 to 30), Lutensole AT grades (C 16 C 18 fatty alcohol ethoxylates, EO units: 11 to 80), Lutensol® ON grades (C 10 oxo alcohol ethoxylates, EO units: 3 to 11) and the Lutensol® TO grades (C 13 OXO alcohol ethoxylates, EO units: 3 to 20) from BASF AG.
• Customary anionic emulsifiers are, for example, alkali metal and ammonium salts of alkyl sulfates (alkyl radical: C 8 to C 12 ), of sulfuric monoesters of ethoxylated alkanols (EO units: 4 to 50, alkyl radical: C 12 to C 18 ) and ethoxylated alkylphenols (EO units: 3 to 50, alkyl radical: C 4 to C 12 ), of alkylsulfonic acids (alkyl radical: C 12 to C 18 ) and of alkylarylsulfonic acids (alkyl radical: C 9 to C 18 ).
• alkyl sulfates alkyl radical: C 8 to C 12
• sulfuric monoesters of ethoxylated alkanols EO units: 4 to 50, alkyl radical: C 12 to C 18
• EO units: 3 to 50 alkyl radical: C 4 to C 12
• alkylsulfonic acids alkyl radical:
• R 1 and R 2 are each H atoms or C 4 -C 24 -alkyl and are not both H atoms, and A and B can be alkali metal ions and/or ammonium ions.
• R 1 and R 2 are preferably linear or branched alkyl radicals having from 6 to 18 carbon atoms, in particular 6, 12 or 16 carbon atoms, or H, with R 1 and R 2 not both being H atoms.
• a and B are preferably sodium, potassium or ammonium, particularly preferably sodium.
• Compounds I in which A and B are each sodium, R 1 is a branched alkyl radical having 12 carbon atoms and R 2 is an H atom or R 1 are particularly advantageous.
• Suitable cation-active emulsifiers are, as a rule, primary, secondary, tertiary or quaternary ammonium salts bearing a C 6 -C 18 -alkyl, C 6 -C 18 -aralkyl or a heterocyclic radical, alkanolammonium salts, pyridinium salts, imidazolinium salts, oxazolinium salts, morpholinium salts, thiazolinium salts and salts of amine oxides, quinolinium salts, isoquinolinium salts, tropylium salts, sulfonium salts and phosphonium salts.
• Examples which may be mentioned are dodecylammonium acetate or the corresponding hydrochloride, the chlorides or acetates of the various 2-(N,N,N-trimethylammonium) ethylparaffinic esters, N-cetylpyridinium chloride, N-laurylpyridinium sulfate and N-cetyl-N,N,N-trimethylammonium bromide, N-dodecyl-N,N,N-trimethylammonium bromide, N-octyl-N,N,N-trimethylammonium bromide, N,N-distearyl-N,N-dimethylammonium chloride and also the gemini surfactant N,N′-(lauryldimethyl)ethylenediamine dibromide.
• nonionic and/or anionic emulsifiers are particularly useful.
• aqueous medium made up of the amounts of deionized water and the dispersant or dispersants.
• solid polymerization catalyst use is frequently made of a support material impregnated or treated with a homogeneous polymerization catalyst.
• Support materials which come into question are generally inert and themselves have no polymerization-catalyzing action. They can be either organic or inorganic in nature.
• Materials which are in particulate form are suitable as organic supports. Activated carbon, cellulose, dextran, dextrose or organic polymers or copolymers are all possible.
• polymers and copolymers are polyolefins such as polyethylene, polypropylene, poly-1-butene and polymethyl-1-pentene and copolymers of monomers on which these polymers are based, also polyesters, polyamides, polyvinyl chloride, polyacrylates and polymethacrylates and polystyrene.
• suitable support materials are copolymers, in particular ternary copolymers, of carbon monoxide and olefinically unsaturated compounds such as ethene, propene or 1-butene, for example carbon monoxide-ethene-propene or carbon monoxide-ethene-1-butene terpolymers.
• the organic support materials which can be used are generally employed as dried polymer powders whose particles preferably have a size in the range from 5 to 300 ⁇ m, often in the range from 10 to 150 ⁇ m or in the range from 30 to 80 ⁇ m.
• the polymeric support systems can be prepared by generally known methods.
• Possible inorganic supports are materials such as silica gel, oxides of aluminum, magnesium, titanium, zirconium, boron, calcium or zinc, aluminosilicates, polysiloxanes, talc, sheet silicates or zeolites.
• Other metal compounds which are sparingly soluble in water, e.g. sparingly soluble metal salts, for example metal sulfates such as barium sulfate and metal sulfides or metal phosphates are suitable as supports.
• Particularly preferred supports are, for example, silica gels, preferably those of the formula SiO 2 a Al 2 O 3 , where a is from 0 to 2, preferably from 0 to 0.5, i.e.
• Suitable silicagels are granular silica gel, for example the commercial product SG 332 from Grace, silylated silica gel obtainable from conventional silica gel by treatment with trimethylchlorosilane, passivated silica gel obtainable by treating conventional silica gel with trialkylaluminums, or spherical silica gel, for example Silicagel® ES 70x from Crosfield.
• Polysiloxanes e.g. the product Deloxane from Degussa
• acidic sheet silicates e.g. the product K10 from Sudchemie
• pyrogenic silicas e.g. finely divided silicas which are usually prepared by flame hydrolysis of silicon tetrachloride in an H 2 /O 2 flame. Pyrogenic silicas have a virtually pore-free surface and have a reduced number of free hydroxy groups.
• silica gels in particular spherical or granular silica gels. These silica gels generally have a mean particle diameter of from 10 to 100 ⁇ m, in particular from 30 to 80 ⁇ m.
• the specific surface area (BET) of the preferred silica gels is generally in the range from 50 to 1000 m 2 /g, in particular in the range from 100 to 400 m 2 /g, and the pore volume is from 0.5 to 5 ml/g, in particular from 1.0 to 3.5 ml/g.
• the support material can be impregnated or treated with the homogeneous polymerization catalyst.
• impregnated means that the homogeneous polymerization catalyst is applied to a nonreactive, inert support material and only physical adsorptive forces exist between the support material and the homogeneous polymerization catalyst.
• treated means that the homogeneous polymerization catalyst is applied to a support material and chemical bonds are formed between the support material and the homogeneous polymerization catalyst. This can be achieved, for example, by modifying the functional groups on the surface of inorganic support materials, e.g. silica gels or aluminum oxides, in a targeted manner.
• silica gels or aluminum oxides can be modified in a targeted manner by treatment with halosilanes, haloboranes, aluminum alkyls or boron alkyls or mixtures thereof or with aminosilanes.
• halosilanes, haloboranes, aluminum alkyls or boron alkyls or mixtures thereof or with aminosilanes can be modified in a targeted manner by treatment with halosilanes, haloboranes, aluminum alkyls or boron alkyls or mixtures thereof or with aminosilanes.
• intermediate forms of the abovementioned polymerization catalysts in which part of the homogeneous polymerization catalyst is chemically bound and the remainder is physically adsorbed on the solid support material are also possible.
• a person skilled in the art will also be familiar with the preparation of a solid polymerization catalyst comprising a solid support material which has been impregnated or treated afterwards with a homogeneous polymerization catalyst (cf., for example, U.S. Pat. No. 5,567,801, U.S. Pat. No. 5,331,083, EP-A 248483, EP-A 404228, EP-A 443687, EP-A 511713, EP-A 559288, EP-A 559289 or EP-A 722968).
• the solid polymerization catalyst is prepared (cf. DE-A 19746280) by, for example,
• the support material can be suspended in the catalyst solution and the solvent can subsequently be removed under reduced pressure.
• nonpolar aprotic liquid solvents are, in particular, linear or branched aliphatic hydrocarbons such as n-pentane, isopentane, hexane, heptane, octane, decane, dodecane, isododecane or mixtures thereof. It is also possible to use industrial mixtures of various hydrocarbons of this type, e.g. kerosene, petroleum ether or Isopar E®. Further nonpolar aprotic liquid media which may be mentioned are cycloaliphatic solvents such as cyclohexane or norbornane. For reasons of availability, preference is given to using n-pentane.
• Suitable polar aprotic liquid solvents include halogenated hydrocarbons such as dichloromethane, dichloroethane or chloroform, aromatic hydrocarbons such as benzene, toluene, ethylbenzene, xylene or chlorobenzene or aliphatic ethers such as tetrahydrofuran or any mixtures of these compounds. It is also possible to use acetonitrile or acetone as liquid polar aprotic solvent or as a component among a plurality of solvents. Preference is given to using acetone, dichloromethane, tetrahydrofuran, acetonitrile or mixtures thereof, in particular dichloromethane.
• liquids or liquid mixtures of differing polarity are immiscible or only very sparingly miscible with one another. This also applies in particular to the respective liquid systems containing dissolved or undissolved reaction constituents such as homogeneous polymerization catalyst or support material.
• the homogeneous polymerization catalysts and the support materials are selected so that the homogeneous polymerization catalysts are sufficiently strongly anchored physically and/or chemically to the solid support material for them not to be leached, or to be leached to only a very minor extent, from the solid support material in the aqueous polymerization medium comprising deionized water and at least one dispersant, even under reaction conditions.
• the homogeneous polymerization catalyst used is a metal complex containing, as metal center, a metal of group VIIIB, IB or IIB of the Periodic Table, for example copper, silver, gold, zinc, cadmium, mercury, iron, cobalt, nickel, ruthenium, rhodium, palladium, osmium, iridium or platinum, preferably iron, cobalt, nickel, ruthenium, rhodium, palladium, osmium, iridium or platinum and particularly preferably cobalt, nickel, ruthenium or palladium.
• Such metal complexes are described, for example, in EP-A 121965, EP-A 743336, WO 96/23010, WO 98/42664, WO 98/42665 or WO 01/10876.
• Such metal complexes frequently become active only as a result of treatment with activators. If this is the case, it is advantageous firstly to prepare the solid polymerization catalyst by impregnating and/or treating the solid support material with the homogeneous polymerization catalyst and to add the activator component to the polymerization mixture comprising deionized water, at least one dispersant and the solid polymerization catalyst only immediately before the polymerization reaction.
• Suitable solid catalysts for the polymerization of monomers according to the present invention are, for example, (1,3-bis(di(n-decyl)phosphino)propane)palladium(II) acetate on silica gel, (1,3-bis(di(n-decyl)phosphino)propane)palladium(II) acetate on activated carbon or (1,3-bis(diphenylphosphino)propane)palladium(II) acetate on silica gel.
• a heterogeneous polymerization catalyst is a solid polymerization catalyst whose solid itself consists essentially of a polymerization-catalyzing composition, as disclosed, for example, in Ziegler et al., Angew. Chem. 1955, 67, pages 541ff.
• cyclic olefins which may be used are cyclopentene, cyclohexene and norbomene, examples of conjugated dienes are butadiene, 2-chlorobutadiene, 2-methylbutadiene and 2,3-dimethylbutadiene and examples of aromatic olefin compounds are styrene, ⁇ -methylstyrene and ortho-, meta- or para-vinyltoluene.
• C 2 -C 20 -1-alkenes are particularly useful.
• the monomers mentioned generally constitute the main monomers which make up a proportion of ⁇ 50% by weight, in particular ⁇ 80% by weight or ⁇ 90% by weight, of the total amount of monomers.
• the monomer mixture to be polymerized frequently consists of 100% by weight of at least one of the abovementioned monomers.
• Reaction products obtained are aqueous polymer dispersions of polyketone compounds.
• the reaction conditions under which the monomers and carbon monoxide are reacted in the presence of a solid polymerization catalyst correspond essentially to the conditions under which monomers and carbon monoxide are polymerized in an aqueous medium in the presence of homogeneously dissolved polymerization catalysts. These conditions are well known to those skilled in the art (cf., for example, DE-A 10061877 or EP-A 121965).
• aqueous polyketone dispersions can be carried out using all solid polymerization catalysts which are able to initiate the formation of polyketones in an aqueous medium. These catalysts are frequently obtained by impregnating or treating a solid support material with a homogeneous hydrolysis-stable polymerization catalyst suitable for the formation of polyketones.
• homogeneous, hydrolysis-stable polymerization catalysts for the preparation of polyketones may be found, for example, in Held et al., Macromolecules 2002, 35, pages 3342 to 3347, and in the patent publications WO 00/63277 and DE-A 10061877.
• Organic solvents which can be used are polar protic or polar aprotic organic compounds having a molecular weight of ⁇ 200 g/mol.
• polar aprotic organic solvents such as halogenated hydrocarbons, for example dichloromethane, dichloroethane or chloroform, aromatic hydrocarbons, for example benzene, toluene, ethylbenzene, xylene or chlorobenzene, or aliphatic ethers such as tetrahydrofuran or any mixtures of these compounds.
• acetonitrile or acetone can be used as liquid polar aprotic solvent or as a component of a plurality of such solvents.
• Polar protic organic solvents are, for example, C 1 -C 10 -alkanols, in particular C 1 -C 6 -alkanols such as methanol, ethanol, n-propanol, isopropanol, 1-butanol, 2-butanol, 2-methyl-2-propanol, and also the corresponding isomeric pentanols, hexanols or heptanols.
• the amount of organic solvent, based on the aqueous medium comprising water and dispersant is often ⁇ 5% by weight, or ⁇ 3% by weight or ⁇ 1% by weight. The polymerization reaction is frequently carried out without addition of organic solvent.
• the amount of the solid polymerization catalyst used for the polymerization is dependent on its activity under the reaction conditions and can be determined by a person skilled in the art in simple preliminary tests. It is economically advantageous for the solid catalysts and the polymerization conditions to be selected so that at least 100 g of polymer are formed from the monomers per gram of solid polymerization catalyst and hour.
• aqueous polymer dispersions obtainable by the polymerization process of the present invention, it is frequently advantageous for these to have a very low content of transition metal compounds [groups VIIIB, IB, IIB of the Periodic Table of the Elements]. It is accordingly advantageous for solid polymerization catalysts whose metal solubility in the aqueous medium is as low as possible to be selected for the polymerization in an aqueous medium.
• a solid support material impregnated or treated with a homogeneous polymerization catalyst is used as solid polymerization catalyst, it is advantageous to select the solid support material, the homogeneous polymerization catalyst and the way in which the homogeneous polymerization catalyst is applied so that the homogeneous polymerization catalyst is firmly anchored to the solid support material.
• the homogeneous polymerization catalyst is particularly advantageous for the homogeneous polymerization catalyst to be sufficiently strongly bound physically and/or chemically to the solid support material for at least 90% by weight, often ⁇ 95% by weight or ⁇ 98% by weight, of the homogeneous catalyst, based on the total amount of homogeneous catalyst on the support material prior to the polymerization reaction, to remain on the support material after a polymerization has been carried out.
• This determination can, for example, be carried out by determining the amount of transition metal from the homogeneous polymerization catalyst on the solid support material before and after the polymerization reaction.
• the concentration of transition metal in the aqueous polymer dispersion can be measured.
• the solid polymerization catalyst is used in the form of particles whose minimum diameter is at least 10 times the weight average diameter of the polymer particles formed by the polymerization. It is advantageous for the minimum diameter or the minimum particle size of the solid polymerization catalyst to differ by a factor of ⁇ 20, ⁇ 50 or ⁇ 100 from the weight average diameter of the polymer particles.
• the preparation of the aqueous polymer dispersion is frequently carried out with exclusion of oxygen, for example under an inert gas atmosphere such as nitrogen or argon or under a carbon monoxide or monomer atmosphere.
• the polymerization temperature and polymerization pressure are strongly dependent on the activity of the solid polymerization catalyst used and the reactivity of the monomers to be reacted.
• the polymerization temperature can be from 0 to 200° C., or from 20 to 150° C. or from 40 to 120° C.
• the polymerization pressure measured in the gas phase can be from 1 to 300 bar, or from 5 to 200 bar or from 10 to 100 bar (in each case absolute values).
• the polymerization reaction of the monomers can in principle be carried out batchwise, semicontinuously or continuously, with or without seed polymer.
• a frequently employed procedure is to place part or all of the deionized water, of the dispersant or dispersants, of the solid polymerization catalyst or catalysts and any seed polymer in a reaction zone under an inert gas atmosphere, heat the mixture to the reaction temperature and add any remaining amount of the abovementioned components, the total amount of the monomers and, if applicable, carbon monoxide to this reaction mixture. It is also possible to add part or all of the monomers or, if applicable, carbon monoxide to the reaction mixture before it is heated to the reaction temperature.
• the monomers can also be introduced into the reaction mixture in the amount in which they are consumed according to the gradient mode of operation known to those skilled in the art.
• the reaction zone is a suitable polymerization reactor such as a stirred vessel, a cascade of stirred vessels, a tube reactor or a loop reactor.
• the aqueous polymer dispersions obtained have contents of polymer solids of from 0.1 to 70% by weight, from 5 to 65% by weight or from 10 to 55% by weight, in each case based on the aqueous polymer dispersion.
• the amount of solid polymerization catalyst used for the polymerization is small, the polymerization catalyst is readily available at low cost or the polymerization catalyst used does not interfere in the later use of the aqueous polymer dispersion because of the composition and size of the catalyst, then the solid polymerization catalyst can frequently be left in the aqueous polymer dispersion. This can be the case when, for example, a finely divided solid polymerization catalyst based on inorganic support materials (e.g.
• titanium dioxide, silicon dioxide or aluminum oxide is used and the same inorganic materials are mixed into the appropriate formulation, for example as pigments or fillers, in the subsequent use of the aqueous polymer dispersion as binder, for example in paints, adhesives, sealants, polymer-based plasters and renders or paper coating compositions.
• the density and/or size of the particles of the solid polymerization catalyst generally differ from the density and/or size of the polymer particles, it can, if necessary, be separated off from the resulting aqueous polymer dispersion in a simple manner by filtration or centrifugation.
• the appropriate process measures are known to those skilled in the art.
• the aqueous polymer dispersion obtained generally has a significantly lower content of transition metal ions than a corresponding aqueous polymer dispersion prepared via homogeneously catalyzed polymerization.
• These aqueous polymer dispersions too, are very useful as binders in adhesives, sealants, polymer-based plasters and renders, paper coating compositions and paints.
• the solid catalyst which has been separated off can be freed of adhering aqueous polymer dispersion by washing with deionized water and be stored in a moist or dry form, frequently under an inert gas such as nitrogen or argon, for a number of weeks or months. It is economically advantageous that this solid polymerization catalyst which has already been used can be used again for further polymerization reactions of monomers in an aqueous medium in the presence of at least one dispersant without a loss in activity, or with only a small loss in activity.
• the present process makes it possible to obtain widely usable aqueous polymer dispersions on the basis of ethylenically unsaturated compounds available at very low cost.
• a technical advantage is that the aqueous polymer dispersions contain no transition metal ions, or only very small amounts of transition metal ions, after the solid polymerization catalysts have been separated off, and an economic advantage is that the solid polymerization catalyst can be reused a number of times.
• the solid pulverulent polymerization catalyst 3 was separated off from the aqueous polymer dispersion by filtration through a porcelain frit (G3). The residue on the filter was washed with deionized water and dried, giving 490 mg of polymerization catalyst.
• the mean copolymer particle diameter was 250 nm.
• the melting point was determined as 150° C.
• the glass transition temperature was 20° C.
• the aqueous copolymer dispersion was stable and displayed no phase separation, precipitates or coagulum formation over a period of 10 weeks.
• the solids content was generally determined by drying about 1 g of the aqueous copolymer dispersion to constant weight in an open aluminum crucible having an internal diameter of about 3 cm in a drying oven at 100° C. and 10 mbar (absolute). To determine the solids content, two separate measurements were carried out in each case and the corresponding mean was calculated.
• the mean particle diameter of the copolymer particles was generally determined by dynamic light scattering on a 0.005-0.01 percent strength by weight aqueous dispersion at 23° C. by means of an Autosizer IIC from Malvern Instruments, UK. The value reported is the mean diameter of the cumulated distribution (cumulant z-average) of the measured autocorrelation function (ISO standard 13321).
• the determination of the glass transition temperature and the melting point was generally carried out in accordance with DIN 53765 by means of a DSC820 instrument, series TA8000 from Mettler-Toledo.
• Polymerization example 1 was repeated using only 450 mg of the solid polymerization catalyst residue from polymerization example 1 in place of 500 mg of fresh solid polymerization catalyst 1 and 1-butene instead of propene.

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